Canonical Allele Identifier: CA338992568
Community Standard Title: NM_000975.5(RPL11):c.158-2A>C
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23693805A>C , CM000663.2:g.23693805A>C GRCh38
NC_000001.10:g.24020295A>C , CM000663.1:g.24020295A>C GRCh37
NC_000001.9:g.23892882A>C NCBI36
NG_011741.1:g.7002A>C
NG_011741.2:g.7027A>C

Transcript Alleles

HGVS Amino-acid Change
NM_000975.5:c.158-2A>C MANE Select NP_000966.2:n.158-2A>C
ENST00000643754.2:c.158-2A>C MANE Select ENSP00000496250.1:n.158-2A>C
NM_000975.3:c.158-2A>C NP_000966.2:n.158-2A>C
NM_001199802.1:c.155-2A>C NP_001186731.1:n.155-2A>C
ENST00000374550.7:c.158-2A>C ENSP00000363676.3:n.158-2A>C
ENST00000374550.8:c.155-2A>C ENSP00000363676.4:n.155-2A>C
ENST00000443624.5:c.152-2A>C ENSP00000390839.1:n.152-2A>C
ENST00000443624.6:n.176-2A>C
ENST00000458455.1:c.152-2A>C ENSP00000398888.1:n.152-2A>C
ENST00000458455.2:c.125-2A>C ENSP00000398888.2:n.125-2A>C
ENST00000467075.2:c.*254-2A>C ENSP00000493634.1:n.*254-2A>C
ENST00000482370.1:n.455-2A>C
ENST00000482370.2:n.152-2A>C